| Literature DB >> 28768176 |
Garron T Dodd1, Zane B Andrews2, Stephanie E Simonds2, Natalie J Michael2, Michael DeVeer3, Jens C Brüning4, David Spanswick2, Michael A Cowley2, Tony Tiganis5.
Abstract
Beige adipocytes can interconvert between white and brown-like states and switch between energy storage versus expenditure. Here we report that beige adipocyte plasticity is important for feeding-associated changes in energy expenditure and is coordinated by the hypothalamus and the phosphatase TCPTP. A fasting-induced and glucocorticoid-mediated induction of TCPTP, inhibited insulin signaling in AgRP/NPY neurons, repressed the browning of white fat and decreased energy expenditure. Conversely feeding reduced hypothalamic TCPTP, to increase AgRP/NPY neuronal insulin signaling, white adipose tissue browning and energy expenditure. The feeding-induced repression of hypothalamic TCPTP was defective in obesity. Mice lacking TCPTP in AgRP/NPY neurons were resistant to diet-induced obesity and had increased beige fat activity and energy expenditure. The deletion of hypothalamic TCPTP in obesity restored feeding-induced browning and increased energy expenditure to promote weight loss. Our studies define a hypothalamic switch that coordinates energy expenditure with feeding for the maintenance of energy balance.Entities:
Keywords: AgRP; Beige adipocyte; Diet-induced thermogenesis; Energy expenditure; Hypothalamus; Insulin; Obesity; Protein tyrosine phosphatase; TCPTP; White adipose tissue browning
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Year: 2017 PMID: 28768176 DOI: 10.1016/j.cmet.2017.07.013
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287